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Structure of 22433-91-6
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2-Bromoisophthalic acid features a bromine substituent at the aromatic ring, enhancing its reactivity in cross-coupling transformations. This ortho-disubstituted benzoic acid derivative offers improved solubility and stability compared to non-halogenated analogs, facilitating efficient incorporation into pharmaceutical intermediates and functional materials under standard conditions.
2-Bromoisophthalic acid serves as a versatile building block in synthetic organic chemistry, enabling direct functionalization at the aromatic ring and carboxylic acid termini. Its bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the ortho-dicarboxylic acid framework supports metal coordination and derivatization for heterocycle synthesis. The compound exhibits good bench stability and is readily purified by recrystallization, making it well-suited for use in medicinal chemistry lead optimization and materials science applications.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: